Record stringlengths 1 197k |
|---|
Design: |
Adult participants will have 4 to 5 visits in 5 years. Children may have up to 12 visits; they may remain in the study up to the age of 23. Most visits will be less than 3 hours. |
Participants will be screened. They will have a physical exam. They will have blood and urine tests. They will complete questionnaires; they will answer questions about their diet, health, and other topics. Some may be referred for additional tests, such as imaging scans and semen analysis. |
Specific tests conducted during study visits will vary, depending on the participant s diagnosis. In addition to repeated blood and urine tests, these may include: |
Body composition measure: Participants will sit in a pod-shaped machine for about 6 minutes. The machines measures the air inside the capsule to record body fat and breathing volume. |
Resting energy expenditure test: Participants will lie down with a clear dome placed over their head. They will breathe quietly for 30 minutes. This test measures the number of calories their body burns at rest. |
... conditions: Hypogonadism conditions: Hypergonadism conditions: Precocious Puberty conditions: Late Puberty conditions: Amenorrhea studyType: OBSERVATIONAL observationalModel: COHORT timePerspective: PROSPECTIVE count: 300 type: ESTIMATED measure: Investigate the relationship between environment, lifestyle, and repr... |
<|newrecord|> nctId: NCT06280794 id: Laser-Bell-2024 briefTitle: Efficacy of Laser Acupuncture for Idiopathic Bell's Palsy overallStatus: COMPLETED date: 2022-03-01 date: 2024-01-01 date: 2024-02-01 date: 2024-02-28 date: 2024-03-29 name: Beijing Tongren Hospital class: OTHER briefSummary: Objective: |
Bell's palsy is characterized by acute, unilateral onset that compromises function and esthetics, exerting a considerable impact on the social, professional, and psychological aspects of the lives of affected individuals. The objective of this study was to determine whether laser acupuncture therapy could relieve sympt... |
Methods: |
This study was randomized controlled trial including 360 patients that undergoing Bell's palsy. All the patients received oral Betahistine Mesylate tablet, Vitamin B1 tablet and Prednisolone. |
Patients were assigned to the laser acupuncture (LA) group, Sham LA group and control group, with 120 patients in each group. LA group and Sham LA group were received 4 weeks of Laser treatment (3 times per week). |
Clinical outcome measure comprised the House-Brackmann grading system, Facial Clinimetric Evaluation Scale (FaCE), Sunnybrook facial grading scale (SBFG), Facial Disability Index (FDI) and Facial Clinimetric Evaluation Scale (FaCE Scale) All the measurements were collected at the baseline, weeks 2, 4, 6, 8, 12 and 24. ... |
<|newrecord|> nctId: NCT06280781 id: 22CX7971 id: NIHR152027 type: OTHER_GRANT domain: National Institute of Health Research - Health Technology Assessment briefTitle: Imperial Prostate 9 - ATLAS (Approaches To Long-Term Active Surveillance) acronym: IP9-ATLAS overallStatus: NOT_YET_RECRUITING date: 2024-07 date: 2029-... |
Research Question P - In patients who are on active surveillance for low to medium risk prostate cancer, I - is the use of regular MRI scans C - compared to current NICE defined standard of care, O - better at detecting cancer progression with less cost to the NHS (fewer PSA tests, biopsies and clinic visits)? |
Patients will be allocated in a 1.1 ratio to either MRI scans or the current NICE defined standard. Randomisation will be blocked (random block size) and stratified by MRI visibility of lesions (3 categories \[ no visible lesion, diffuse changes, discrete visible lesion\]), cancer Grade Group (GG1, GG2) and time since ... |
PSA 3 monthly in year 1 and then 6 monthly with rectal exam annually. MRI will be carried out at 12 months (if not had one at diagnosis). A biopsy will be required if indicated due to changes in rectal exam or PSA. |
Planned (Regular MRI based active surveillance): |
Patients with a visible lesion or medium risk cancer will have PSA 6 monthly and MRI annually. All other patients will undergo PSA 6 monthly and MRI in years 1, 3 and 5. In all patients, a targeted biopsy will be carried out if the MRI PRECISE score is \>/=4. primaryPurpose: OTHER masking: NONE count: 1263 type: ESTIMA... |
<|newrecord|> nctId: NCT06280768 id: SHR-2004-102 briefTitle: Study on the Safety and Tolerability, Pharmacokinetics and Pharmacodynamics of SHR-2004 Injection in Adult Patients With Atrial Fibrillation overallStatus: NOT_YET_RECRUITING date: 2024-03-01 date: 2024-12-31 date: 2024-12-31 date: 2024-02-28 date: 2024-02-2... |
<|newrecord|> nctId: NCT06280755 id: ICO-S-002 briefTitle: Clinical Impact Through AI-assisted MS Care - A Retrospective Multi-center Observational Study. acronym: RECLAIM overallStatus: NOT_YET_RECRUITING date: 2024-03 date: 2027-04 date: 2027-04 date: 2024-02-28 date: 2024-02-28 name: icometrix class: INDUSTRY name: ... |
<|newrecord|> nctId: NCT06280742 id: APHP221366 briefTitle: Study of Neuroinflammation in Multiple Sclerosis by PET-MRI Imaging Using the Radiotracer ([18F]-DPA-714) : a Multicentre Cohort Study (INFLANET) acronym: INFLANET overallStatus: NOT_YET_RECRUITING date: 2024-07-01 date: 2026-03-01 date: 2026-03-01 date: 2024-... |
The objectives of the INFLANET project are (1) to conduct the first multicenter study assessing neuroinflammation in patients with active MS using \[18F\]DPA-714 PET tracer, and (2) to establish a methodology suitable for the quantification of multicenter PET data obtained with \[18F\]DPA-714. The INFLANET initiative a... |
<|newrecord|> nctId: NCT06280729 id: AI-TRYDIA briefTitle: AI-Predicted Disease Trajectories in Diabetes: A Retrospective Study acronym: AI-TRYDIA overallStatus: NOT_YET_RECRUITING date: 2024-03-01 date: 2025-03-01 date: 2026-03-01 date: 2024-02-28 date: 2024-02-28 name: IRCCS San Raffaele class: OTHER briefSummary: Th... |
<|newrecord|> nctId: NCT06280716 id: 18817 id: J2T-MC-KGBW type: OTHER domain: Eli Lilly and Company briefTitle: A Study of Lebrikizumab (LY3650150) With/Without Topical Corticosteroid Treatment in Participants With Moderate-to-Severe Atopic Dermatitis overallStatus: NOT_YET_RECRUITING date: 2024-05-06 date: 2025-12-17... |
<|newrecord|> nctId: NCT06280703 id: 18792 id: J4P-MC-IYAB type: OTHER domain: Eli Lilly and Company id: U1111-1301-8386 type: OTHER domain: Universal Trial Number id: 2023-510365-10-00 type: OTHER domain: EU Trial Number briefTitle: A Study of LY3938577 in Healthy Participants and Participants With Type 1 Diabetes Mel... |
The study will also evaluate the safety and tolerability of LY3938577 and information about any side effects experienced will be collected. |
The study will be conducted in three parts (A, B, and C). Healthy participants in part A will receive one single dose of LY3938577 or a placebo, whereas participants in Parts B and C with T1DM will receive single doses of either LY3938577 or Insulin Deglude given via intravenous (IV) infusion. |
The study will last up to approximately 5.5, 10 and 13 weeks for parts A, B, and C, respectively, including screening period. conditions: Healthy conditions: Type 1 Diabetes Mellitus studyType: INTERVENTIONAL phases: PHASE1 allocation: RANDOMIZED interventionModel: CROSSOVER interventionModelDescription: Parallel (Part... |
<|newrecord|> nctId: NCT06280690 id: NL83765.058.23 briefTitle: SGM-101 Tumor Targeted Fluorescence Endoscopy in Rectal Polyps With Suspected T1 Adenocarcinoma or High Grade Dysplasia acronym: SGM-T1 overallStatus: RECRUITING date: 2024-01-31 date: 2025-04-30 date: 2025-07-30 date: 2024-02-28 date: 2024-02-29 name: Lei... |
<|newrecord|> nctId: NCT06280677 id: 2023.Aurora-Donor briefTitle: Aurora Test for ART Donor Patients (AURORA-Donor) overallStatus: RECRUITING date: 2024-02-16 date: 2025-04 date: 2025-09 date: 2024-02-28 date: 2024-02-28 name: Fertiga, Belgium class: INDUSTRY name: Fertilab name: Ferring Pharmaceuticals briefSummary: ... |
<|newrecord|> nctId: NCT06280664 id: IRB20-1151 briefTitle: Efficacy Of Hiatal Closure For GERD overallStatus: RECRUITING date: 2020-10-02 date: 2024-10 date: 2024-10 date: 2024-02-28 date: 2024-02-28 name: University of Chicago class: OTHER briefSummary: The purpose of this protocol is to study the efficacy of hiatal ... |
<|newrecord|> nctId: NCT06280651 id: RGP 2/348/44 id: RGP 2/348/44 type: OTHER_GRANT domain: kING kHALID UNIVERSITY briefTitle: Dietary Impacts on Oral Health in Autistic Children: A Cross-Sectional Analysis acronym: OHIDPAP-CS overallStatus: NOT_YET_RECRUITING date: 2024-03-25 date: 2024-04-30 date: 2024-05-15 date: 2... |
<|newrecord|> nctId: NCT06280638 id: 2023-2095 briefTitle: CT-derived Virtual Stenting Optimize Coronary Revascularization (CT-COMPASS) acronym: CT-COMPASS overallStatus: NOT_YET_RECRUITING date: 2024-02 date: 2024-12 date: 2025-12 date: 2024-02-28 date: 2024-02-28 name: China National Center for Cardiovascular Disease... |
Computed tomography (CT) coronary physiology-derived virtual stenting (CT-VS) based on pre-PCI CCTA angiograms is an augmented reality (AR) approach that simulates the post-stenting physiology assuming that the specified segment of the treated vessel is successfully dilated by implanting virtual stents. Previous studie... |
However, there is a lack of knowledge regarding the efficacy of this novel physiological index that is available pre-PCI in achieving final post-PCI optimal physiological result. The Trials of "Computed Tomography Coronary Physiology-derived Virtual Stenting Guided Revascularization Strategy in Patients with Coronary A... |
<|newrecord|> nctId: NCT06280625 id: 24388 briefTitle: The Effect of the Inclusion of Soybean Flour on Glycemic Responses overallStatus: RECRUITING date: 2024-03-01 date: 2025-02-28 date: 2025-03-25 date: 2024-02-28 date: 2024-02-28 name: University of Illinois at Urbana-Champaign class: OTHER name: Kenneth Dallmier Co... |
In many regions of Latin America, as well as in the Middle East and North Africa (MENA) regions, bread is the staple source of calories, but it is a relatively poor source of balanced nutrition. Bread enriched with soy flour could provide higher dietary protein while moderating blood glucose (and insulin) spikes, which... |
<|newrecord|> nctId: NCT06280612 id: RCS10042023 briefTitle: The Effect of Live Cat and Simulation Cat Therapies on Oncology Patients overallStatus: COMPLETED date: 2023-06-01 date: 2023-07-15 date: 2023-09-01 date: 2024-02-28 date: 2024-03-01 name: Karadeniz Technical University class: OTHER briefSummary: It is known ... |
<|newrecord|> nctId: NCT06280599 id: SON KMU briefTitle: Transitional Care Model for Patients With Stroke overallStatus: RECRUITING date: 2023-09-01 date: 2024-04-01 date: 2024-04-29 date: 2024-02-28 date: 2024-04-03 name: Kaohsiung Medical University class: OTHER briefSummary: Patients with stroke benefitted from supe... |
<|newrecord|> nctId: NCT06280586 id: 44/21 briefTitle: Effectiveness of Intervention in Prevention of Sarcopenia, Frailty and Functional Decline in Pre-frail Community Elderly acronym: ESPAI-F overallStatus: ACTIVE_NOT_RECRUITING date: 2021-11-15 date: 2023-10-30 date: 2024-12-31 date: 2024-02-28 date: 2024-02-28 name:... |
The aim of this study is to evaluate the safety and effectiveness of an intervention based on the control of chronic diseases, a good use of medicines, diet, physical exercise and good social support, in the prevention . of frailty in old people who are at risk of frailty. |
These criteria for participating in the study are why we invite you to participate. Your participation is voluntary. Your decision to participate or not in the study will not affect the medical care you may need. Before making a decision, read this information sheet carefully and ask the person who informs you the ques... |
In the study there will be two groups, one will receive the study intervention and the other will not receive any special treatment (we call it the control group). The assignment of each individual to one group or the other will take place once you have decided to participate. This assignment will be made at random so ... |
<|newrecord|> nctId: NCT06280573 id: MS1 briefTitle: COld Exposure With Controlled BReathing And Meditation in Patients With Multiple Sclerosis (COBRAMS) acronym: COBRAMS overallStatus: ACTIVE_NOT_RECRUITING date: 2022-09-01 date: 2025-12-01 date: 2025-12-01 date: 2024-02-28 date: 2024-03-19 name: Comenius University c... |
Researchers will compare the effect to control groups of MS patients without intervention. conditions: Multiple Sclerosis studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED interventionModel: PARALLEL primaryPurpose: TREATMENT masking: SINGLE whoMasked: OUTCOMES_ASSESSOR count: 50 type: ESTIMATED name: Wim Hof... |
<|newrecord|> nctId: NCT06280560 id: 2109-FIVI-087-FD id: PI23/00860 type: OTHER_GRANT domain: Instituto de Salud Carlos III, co-funded by European Union briefTitle: Impact of IVF Hormonal Therapy on Endometrial Receptivity and Endometrial Senescent Cell Pathological Accumulation acronym: HormoSenoRec overallStatus: RE... |
We hypothesize that the supraphysiologic hormone levels required for both COS+LPS, and HRT may be inducing alterations in endometrial composition and function, specifically the chronic accumulation of senescent cells; either due to an excessive hormonal induction, a lack of clearance due to a deficit of uNKs, or a comb... |
The in vitro clearance of endometrial senescent cells by selective induction of apoptosis has been found to enhance the decidualization capacity of the rest of Endometrial Stromal Cells (EnSC), which could represent in a future adjuvant strategy to reduce the potentially deleterious effects of supraphysiologic hormone ... |
The results derived from this project would have a direct impact on clinical practice. First, the results would allow us to evaluate, based on experimental data, potential endometrial side effects of stimulation protocols commonly used in IVF treatments. In addition, in the case of finding a pathological accumulation o... |
<|newrecord|> nctId: NCT06280547 id: CUP 13-2 id: Cairo university type: OTHER domain: Cairo University briefTitle: The Effect of Oral Health Education on Knowledge, Attitude, Practice and Dental Caries Among Egyptian School Children acronym: KAP overallStatus: NOT_YET_RECRUITING date: 2024-02-29 date: 2024-03-02 date:... |
<|newrecord|> nctId: NCT06280534 id: XT1061-2022-01 briefTitle: Safety, Tolerability Phase Ia Study of XT1061 in Single and Multiple Doses in Healthy Subjects acronym: XT1061 overallStatus: RECRUITING date: 2023-07-18 date: 2024-02-29 date: 2024-03-31 date: 2024-02-28 date: 2024-02-28 name: Xi'an Xintong Pharmaceutical... |
<|newrecord|> nctId: NCT06280521 id: 38RC23.0331 briefTitle: Validation of the Girls Questionnaire for Autism Spectrum Condition in French Langage acronym: fGQ-ASC overallStatus: NOT_YET_RECRUITING date: 2024-04 date: 2026-04 date: 2026-05 date: 2024-02-28 date: 2024-02-28 name: University Hospital, Grenoble class: OTH... |
The GQ-ASC is presented as a self-questionnaire with 29 items which assess clinical characteristics specific to the adult female presentation of ASD in the dimensions (five) of imagination and play, camouflage, sensoriality, social situations and interests. To date, several studies have relevantly used the GQ-ASC in po... |
The main objective of this online study is therefore to measure the predictive validity of the French version of the Girl Questionnaire for Autism Spectrum Conditions (fGQ-ASC) for the diagnosis of ASD in adult women over 18 years of age and speaking French kindergarten. Subjects included in this online study will comp... |
<|newrecord|> nctId: NCT06280508 id: SYSKY-2024-082-01 briefTitle: Chemotherapy Combined With Adebrelimab and Apatinib as the Perioperative Treatment in Patients With Biliary Tract Cancer overallStatus: RECRUITING date: 2024-03-01 date: 2027-03-31 date: 2028-03-31 date: 2024-02-28 date: 2024-04-23 name: Sun Yat-Sen Mem... |
<|newrecord|> nctId: NCT06280495 id: INTENSIFY-CRC briefTitle: Neoadjuvant Serplulimab & Bevacizumab With FOLFOX vs. FOLFOX Alone in RAS/BRAF WT, pMMR/MSS CRC Patients overallStatus: RECRUITING date: 2024-02-01 date: 2026-12-31 date: 2028-12-31 date: 2024-02-28 date: 2024-03-04 name: Sun Yat-sen University class: OTHER... |
<|newrecord|> nctId: NCT06280482 id: HSC-MS-23-0332 briefTitle: Nicotinamide Riboside (NR) to Treat Moyamoya-like Cerebrovascular Disease in Smooth Muscle Dysfunction Syndrome (SMDS) overallStatus: RECRUITING date: 2024-03-06 date: 2025-07-25 date: 2025-07-25 date: 2024-02-28 date: 2024-04-05 name: The University of Te... |
<|newrecord|> nctId: NCT06280469 id: KY20232298-C-1 briefTitle: Single-operator Versus Double-operator in Single-Balloon Enteroscopy acronym: SBE overallStatus: RECRUITING date: 2024-01-01 date: 2025-12 date: 2025-12 date: 2024-02-28 date: 2024-02-28 name: Shuhui Liang class: OTHER briefSummary: Compared with two-perso... |
<|newrecord|> nctId: NCT06280456 id: 2023-09-017A briefTitle: Tranexamic Acid Injection With Different Drainage Clamping Time After Anterior Cruciate Ligament Reconstruction overallStatus: COMPLETED date: 2022-09-05 date: 2023-01-05 date: 2023-02-05 date: 2024-02-28 date: 2024-02-28 name: Taipei Veterans General Hospit... |
<|newrecord|> nctId: NCT06280443 id: CE22407B briefTitle: Sarcopenia in Chronic Lung Diseases overallStatus: RECRUITING date: 2022-11-25 date: 2024-10-13 date: 2032-09-30 date: 2024-02-28 date: 2024-04-04 name: Taichung Veterans General Hospital class: OTHER briefSummary: Inclusion criteria A)Outpatients with COPD (chr... |
B) Patients who agree to provide the ID card number to the research team for usage as a link to the National Health Insurance research database and Health bank to explore the continuity of care and the use of medical resources conditions: Sarcopenia conditions: COPD conditions: Asthma conditions: ILD studyType: OBSERVA... |
<|newrecord|> nctId: NCT06280430 id: Vascular affection in behcet briefTitle: Vascular Affection in Behcet Disease overallStatus: NOT_YET_RECRUITING date: 2024-03-01 date: 2025-03-01 date: 2025-04-01 date: 2024-02-28 date: 2024-02-28 name: Assiut University class: OTHER briefSummary: To measure the level of serum elafi... |
<|newrecord|> nctId: NCT06280417 id: Unreamed IMN In IIIa tibia briefTitle: Unreamed Intramedullary Tibial Nailing in Treatment of Open IIIa Diaphyseal Tibial Fractures in Adults overallStatus: NOT_YET_RECRUITING date: 2024-06-01 date: 2025-06-01 date: 2025-08-01 date: 2024-02-28 date: 2024-02-28 name: Assiut Universit... |
<|newrecord|> nctId: NCT06280404 id: Body first in lap chole briefTitle: Body First Approach in Lap Cholecystectomy in Cases With Obscure Calot's Triangle overallStatus: NOT_YET_RECRUITING date: 2024-03-15 date: 2025-03-15 date: 2025-08-08 date: 2024-02-28 date: 2024-02-28 name: Assiut University class: OTHER briefSumm... |
<|newrecord|> nctId: NCT06280391 id: ACT18018 id: U1111-1295-3237 type: REGISTRY domain: ICTRP id: 2023-508663-70 type: REGISTRY domain: CTIS briefTitle: A Proof-of-Concept Study to Assess the Efficacy, Safety and Tolerability of Itepekimab (Anti-IL-33 mAb) in Participants With Non-cystic Fibrosis Bronchiectasis overal... |
Study details include: |
* The study duration (screening, 24-52-week treatment, 20-week safety follow-up) will be up to 47-77 weeks. |
* The treatment duration will be up to 24-52 weeks. |
* The follow-up duration will be 20 weeks. |
* Site/phone visits are at a monthly interval. conditions: Bronchiectasis studyType: INTERVENTIONAL phases: PHASE2 allocation: RANDOMIZED interventionModel: PARALLEL primaryPurpose: TREATMENT masking: TRIPLE whoMasked: PARTICIPANT whoMasked: CARE_PROVIDER whoMasked: INVESTIGATOR count: 300 type: ESTIMATED name: Itepeki... |
<|newrecord|> nctId: NCT06280378 id: CP-KL003-003/01 briefTitle: A Phase I/II Clinical Study of the KL003 Cell Injection in β-Thalassemia Major Participants overallStatus: NOT_YET_RECRUITING date: 2024-02 date: 2025-05 date: 2027-05 date: 2024-02-28 date: 2024-02-28 name: Kanglin Biotechnology (Hangzhou) Co., Ltd. clas... |
<|newrecord|> nctId: NCT06280365 id: 012 briefTitle: MWM Technique in Patients With Knee OA overallStatus: COMPLETED date: 2024-02-19 date: 2024-03-15 date: 2024-03-15 date: 2024-02-28 date: 2024-04-03 name: Okan University class: OTHER briefSummary: The aim of this study is to investigate the effect of the MWM techniq... |
<|newrecord|> nctId: NCT06280352 id: AUVA_Knieathlon_2024 briefTitle: Robotic Assisted vs Custom Made Total Knee Arthroplasty acronym: Knieathlon overallStatus: RECRUITING date: 2024-03-01 date: 2024-12 date: 2026-12 date: 2024-02-28 date: 2024-03-12 name: Austrian Workers Compensation Board Styria class: OTHER briefSu... |
* Which implant/philosophy yields better clinical outcomes? |
* Which implant/philosophy yields better satisfaction? |
* Which system is more OR efficient? Participants will be followed for 2 years postoperatively. conditions: Knee Osteoarthritis studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED interventionModel: PARALLEL interventionModelDescription: Randomized primaryPurpose: TREATMENT masking: DOUBLE whoMasked: PARTICIPAN... |
<|newrecord|> nctId: NCT06280339 id: IRB23-0190 briefTitle: Food Cravings Strategies During Dietary Weight Loss overallStatus: RECRUITING date: 2024-01-29 date: 2024-06-01 date: 2024-08-01 date: 2024-02-28 date: 2024-02-28 name: University of Illinois at Urbana-Champaign class: OTHER briefSummary: The purpose is to opt... |
The objective of this study is to determine the efficacy of craving coping strategies on weight loss outcomes by conducting a randomized controlled trial. Participants will be randomized to receive one of the two strategies to manage food cravings. conditions: Obesity conditions: Food Cravings conditions: Weight Loss s... |
<|newrecord|> nctId: NCT06280326 id: Orogastric Tube Removal briefTitle: Effect of Different Materials Used in Orogastric Tube Removal on Skin Condition in Premature Babies overallStatus: ACTIVE_NOT_RECRUITING date: 2024-02-05 date: 2024-06-05 date: 2024-08-05 date: 2024-02-28 date: 2024-02-28 name: Ondokuz Mayıs Unive... |
<|newrecord|> nctId: NCT06280313 id: uHCC-STI-TJ01 briefTitle: Impact of Splenectomy on the Efficacy of Targeted Therapy and Immunotherapy in Unresectable HCC Patients With Cirrhotic Portal Hypertension overallStatus: RECRUITING date: 2024-03-15 date: 2027-03-15 date: 2028-03-15 date: 2024-02-28 date: 2024-04-10 name: ... |
<|newrecord|> nctId: NCT06280300 id: UVMMC2203 briefTitle: Multi-disciplinary Care for Brain Metastases overallStatus: RECRUITING date: 2023-11-16 date: 2024-11-01 date: 2025-11-01 date: 2024-02-28 date: 2024-02-28 name: University of Vermont Medical Center class: OTHER briefSummary: This is a health services intervent... |
<|newrecord|> nctId: NCT06280287 id: FAPI-PLAQUE briefTitle: PET Imaging of Fibroblast Activation in Atherosclerosis overallStatus: RECRUITING date: 2021-08-01 date: 2024-12-31 date: 2025-12-31 date: 2024-02-28 date: 2024-02-28 name: Peking Union Medical College Hospital class: OTHER briefSummary: Fibroblast activation... |
<|newrecord|> nctId: NCT06280274 id: STUDY00025798 briefTitle: Metformin Use in Patients Undergoing Total Joint Replacement Surgery overallStatus: NOT_YET_RECRUITING date: 2024-02-26 date: 2025-05-30 date: 2025-05-30 date: 2024-02-28 date: 2024-03-01 name: Oregon Health and Science University class: OTHER briefSummary:... |
The primary objective of this study is to assess the feasibility of conducting a large, randomized trial with regards to timely recruitment, study drug administration, protocol adherence, and overall retention in patients undergoing total joint arthroplasty. |
Secondarily, the investigators aim to obtain preliminary estimates of group-specific outcome means and variances for primary and secondary outcomes of a larger future trial. conditions: Hyperglycemia studyType: INTERVENTIONAL phases: PHASE4 allocation: RANDOMIZED interventionModel: PARALLEL interventionModelDescription... |
<|newrecord|> nctId: NCT06280261 id: GO20/296 briefTitle: The Struggle That Is Phenylketonuria : What Do The Patients and Caregivers Suffer From overallStatus: COMPLETED date: 2020-05-27 date: 2020-09-01 date: 2020-09-01 date: 2024-02-28 date: 2024-02-28 name: Hacettepe University class: OTHER briefSummary: Objective: ... |
<|newrecord|> nctId: NCT06280248 id: EUS in pancreatic fluid briefTitle: EUS Guided Drainage of Post Pancreatitis Pancreatic Fluid Collection overallStatus: NOT_YET_RECRUITING date: 2024-03 date: 2026-03 date: 2026-06 date: 2024-02-28 date: 2024-02-28 name: Assiut University class: OTHER briefSummary: The number as wel... |
* Assess the technical success rates, clinical success rates and potential complications of the different techniques for the best drainage of PFCs as regard type, caliber and number of plastic stents and ideal timing for stent removal. |
* Compare between early vs late intervention for complete endoscopic necrosectomy of WOPN as regard technical success rates, clinical success rates, potential complications and number of sessions needed. conditions: Pancreas Pseudocyst studyType: INTERVENTIONAL phases: NA allocation: NA interventionModel: SINGLE_GROUP ... |
<|newrecord|> nctId: NCT06280235 id: 1447-0005 id: U1111-1297-3126 type: REGISTRY domain: WHO International Clinical Trials Registry Platform (ICTRP) id: 2023-507942-10-00 type: REGISTRY domain: CTIS briefTitle: A Study to Test Different Doses of BI 1569912 in People With Depression Who Take Anti-depressive Medicine ov... |
Participants continue their standard therapy throughout the study. |
Participants are put into 4 groups by chance. 3 of the 4 groups take different doses of BI 1569912. 1 group takes placebo. Placebo tablets looks like BI 1569912 but do not contain any medicine. Participants take the tablets once a day for 6 weeks. |
Participants are in the study for about 2 to 4 and a half months. During this time, they visit the study site at least 6 times. At the visits, doctors ask participants about their symptoms. |
The participants answer questions about their depression symptoms. The results are compared between the groups. The doctors also regularly check the general health of participants. conditions: Depressive Disorder, Major studyType: INTERVENTIONAL phases: PHASE2 allocation: RANDOMIZED interventionModel: PARALLEL primaryP... |
<|newrecord|> nctId: NCT06280222 id: VR FOR ANXIETY-HMO-CTIL briefTitle: The Effectiveness of Virtual Reality on Anxiety Reduction in Women Undergoing Elective Egg Cryopreservation. acronym: VRFORANXIETY overallStatus: RECRUITING date: 2023-11-15 date: 2024-11-15 date: 2025-02-01 date: 2024-02-28 date: 2024-02-28 name:... |
<|newrecord|> nctId: NCT06280209 id: 351-201 id: 2023-506737-30-00 type: OTHER domain: EU CT briefTitle: A Phase 1/2 Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of BMN 351 in Participants With Duchenne Muscular Dystrophy overallStatus: RECRUITING date: 2024-01-03 date: 2025-12 date:... |
<|newrecord|> nctId: NCT06280196 id: BAT-3306-002-CR briefTitle: A Study to Evaluate PK, Efficacy, and Safety of BAT3306 Plus Chemo and Compare With Keytruda®(EU/US) in Participants With IV nqNSCLC overallStatus: NOT_YET_RECRUITING date: 2024-08-15 date: 2027-07-30 date: 2028-10-30 date: 2024-02-28 date: 2024-03-25 nam... |
<|newrecord|> nctId: NCT06280183 id: 323132 briefTitle: Functional Inspiratory Muscle Training in Obese Individuals overallStatus: NOT_YET_RECRUITING date: 2024-02-28 date: 2025-06-30 date: 2025-06-30 date: 2024-02-28 date: 2024-02-28 name: Biruni University class: OTHER name: Istanbul Galata University briefSummary: I... |
This study aims to investigate the effects of functional inspiratory muscle training on body composition, cardiometabolic markers, functional capacity, respiratory function, respiratory muscle strength, and respiratory muscle performance in obese individuals. conditions: Obesity studyType: INTERVENTIONAL phases: NA all... |
Subsets and Splits
No community queries yet
The top public SQL queries from the community will appear here once available.